These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

228 related articles for article (PubMed ID: 18029128)

  • 1. Discrepancy between auditory brainstem responses, auditory steady-state responses, and auditory behavior in two patients with Pelizaeus-Merzbacher disease.
    Tanaka M; Hamano S; Sakata H; Adachi N; Kaga K; Osaka H; Kurosawa K
    Auris Nasus Larynx; 2008 Sep; 35(3):404-7. PubMed ID: 18029128
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.
    Kuan CC; Sano M; Kaga K; Kodama M; Kodama K
    Acta Otolaryngol; 2008 May; 128(5):539-46. PubMed ID: 18421608
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Development of speech and hearing of two children with Pelizaeus-Merzbacher disease presenting only waves I and II of the auditory brainstem response.
    Rikitake M; Kaga K
    Acta Otolaryngol; 2012 May; 132(5):563-9. PubMed ID: 22264126
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comparison of auditory steady-state responses and auditory brainstem responses in audiometric assessment of adults with sensorineural hearing loss.
    Lin YH; Ho HC; Wu HP
    Auris Nasus Larynx; 2009 Apr; 36(2):140-5. PubMed ID: 18620826
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Duplication of the PLP gene and the classical form of Pelizaeus-Merzbacher disease].
    Blanco-Barca MO; Eirís-Puñal J; Soler-Regal C; Castro-Gago M
    Rev Neurol; 2003 Sep 1-15; 37(5):436-8. PubMed ID: 14533091
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Variable expression of a novel PLP1 mutation in members of a family with Pelizaeus-Merzbacher disease.
    Fattal-Valevski A; DiMaio MS; Hisama FM; Hobson GM; Davis-Williams A; Garbern JY; Mahoney MJ; Kolodny EH; Pastores GM
    J Child Neurol; 2009 May; 24(5):618-24. PubMed ID: 19151366
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Meta-analysis of variables that affect accuracy of threshold estimation via measurement of the auditory steady-state response (ASSR).
    Tlumak AI; Rubinstein E; Durrant JD
    Int J Audiol; 2007 Nov; 46(11):692-710. PubMed ID: 17978952
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Development of tone-pip auditory brainstem responses and auditory steady-state responses in infants aged 0-6 months.
    Qian L; Yi W; Xingqi L; Yinsheng C; Wenying N; Lili X; Yinghui L
    Acta Otolaryngol; 2010 Jul; 130(7):824-30. PubMed ID: 20092381
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Degree of hypomyelination and magnetic resonance spectroscopy findings in patients with Pelizaeus Merzbacher phenotype.
    Plecko B; Stöckler-Ipsiroglu S; Gruber S; Mlynarik V; Moser E; Simbrunner J; Ebner F; Bernert G; Harrer G; Gal A; Prayer D
    Neuropediatrics; 2003 Jun; 34(3):127-36. PubMed ID: 12910435
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplications.
    Shimojima K; Inoue T; Hoshino A; Kakiuchi S; Watanabe Y; Sasaki M; Nishimura A; Takeshita-Yanagisawa A; Tajima G; Ozawa H; Kubota M; Tohyama J; Sasaki M; Oka A; Saito K; Osawa M; Yamamoto T
    Brain Dev; 2010 Mar; 32(3):171-9. PubMed ID: 19328639
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sedation for children 2 to 5 years of age undergoing auditory brainstem response and auditory steady state responses recordings.
    François M; Teissier N; Barthod G; Nasra Y
    Int J Audiol; 2012 Apr; 51(4):282-6. PubMed ID: 21936745
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical neurophysiology in GJA12-related hypomyelination vs Pelizaeus-Merzbacher disease.
    Henneke M; Gegner S; Hahn A; Plecko-Startinig B; Weschke B; Gärtner J; Brockmann K
    Neurology; 2010 Jun; 74(22):1785-9. PubMed ID: 20513814
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A severe connatal form of Pelizaeus Merzbacher disease in a Czech boy caused by a novel mutation (725C>A, Ala242Glu) at the 'jimpy(msd) codon' in the PLP gene.
    Seeman P; Paderova K; Benes V; Sistermans EA
    Int J Mol Med; 2002 Feb; 9(2):125-9. PubMed ID: 11786921
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Three young adult patients with Pelizaeus-Merzbacher disease who showed only waves I and II in auditory brainstem responses but had good auditory perception.
    Kaga K; Tamai F; Kodama M; Kodama K
    Acta Otolaryngol; 2005 Sep; 125(9):1018-23. PubMed ID: 16193596
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Reliability of brain stem audiometry in specific learning disorders (disorders of sensory integration)].
    von Deuster C; Axmann D
    Laryngorhinootologie; 1995 Sep; 74(9):539-42. PubMed ID: 7495434
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Classic Pelizaeus-Merzbacher disease in a girl with an unbalanced chromosomal translocation and functional duplication of PLP1.
    Yiu EM; Farrell SA; Soman T
    Mov Disord; 2009 Oct; 24(14):2171-2. PubMed ID: 19705472
    [No Abstract]   [Full Text] [Related]  

  • 17. Compensating for central nervous system dysmyelination: females with a proteolipid protein gene duplication and sustained clinical improvement.
    Inoue K; Tanaka H; Scaglia F; Araki A; Shaffer LG; Lupski JR
    Ann Neurol; 2001 Dec; 50(6):747-54. PubMed ID: 11761472
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reduced PLP1 expression in induced pluripotent stem cells derived from a Pelizaeus-Merzbacher disease patient with a partial PLP1 duplication.
    Shimojima K; Inoue T; Imai Y; Arai Y; Komoike Y; Sugawara M; Fujita T; Ideguchi H; Yasumoto S; Kanno H; Hirose S; Yamamoto T
    J Hum Genet; 2012 Sep; 57(9):580-6. PubMed ID: 22695888
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of proteolipid protein 1 gene duplication by multiplex ligation-dependent probe amplification: first report of genetically confirmed family of Pelizaeus-Merzbacher disease in Korea.
    Kim SJ; Yoon JS; Baek HJ; Suh SI; Bae SY; Cho HJ; Ki CS
    J Korean Med Sci; 2008 Apr; 23(2):328-31. PubMed ID: 18437021
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects.
    Vaurs-Barrière C; Deville M; Sarret C; Giraud G; Des Portes V; Prats-Viñas JM; De Michele G; Dan B; Brady AF; Boespflug-Tanguy O; Touraine R
    Ann Neurol; 2009 Jan; 65(1):114-8. PubMed ID: 19194886
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.